(Q34085583)

30 July 2017

1 reference

title

Does failure of parkin-mediated ubiquitination cause juvenile parkinsonism? (English)

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30 July 2017

protein ubiquitination

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1 reference

3

C Haass

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30 July 2017

P J Kahle

1

1 reference

PubMed ID

11084358

30 July 2017

U Leimer

series ordinal

2

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30 July 2017

1 November 2000

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30 July 2017

4

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Trends in Biochemical Sciences

inferred from page(s)

published in

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30 July 2017

25

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30 July 2017

524-527

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30 July 2017

11

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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

30 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Alpha-synuclein in Lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

The ubiquitin pathway in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Association between early-onset Parkinson's disease and mutations in the parkin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

A Drosophila model of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Dopaminergic loss and inclusion body formation in alpha-synuclein mice: implications for neurodegenerative disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Neuropathology in mice expressing human alpha-synuclein

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Subcellular localization of wild-type and Parkinson's disease-associated mutant alpha -synuclein in human and transgenic mouse brain

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

alpha-Synuclein immunoreactivity in dementia with Lewy bodies: morphological staging and comparison with ubiquitin immunostaining

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

1 reference

7 January 2021

The ubiquitin-conjugating enzymes UbcH7 and UbcH8 interact with RING finger/IBR motif-containing domains of HHARI and H7-AP1

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

1 reference

7 January 2021

A novel ubiquitination factor, E4, is involved in multiubiquitin chain assembly.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2800%2901682-0

7 January 2021

10.1016/S0968-0004(00)01682-0

Identifiers

DOI

1 reference

30 July 2017

1 reference

PubMed ID

11084358